Variants in gene KIF1A with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_001244008.2(KIF1A):c.223C>T (p.Arg75Trp)	rs778224699	0.00004
NM_001244008.2(KIF1A):c.647G>C (p.Arg216Pro)	rs672601368
NM_001244008.2(KIF1A):c.947G>A (p.Arg316Gln)	rs749718096

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